Epi De France recalls specific bread products due to undeclared peanut and tree nut residue in wheat gluten. Consumers should check product labels for the affected items and contact the company for details.
Undeclared allergen: Bread products were manufactured using raw material (wheat gluten) that was recalled due to undeclared peanut and/or tree nut residue.
Epi De France is recalling certain bread products because they contain undeclared peanut and/or tree nut residue from wheat gluten. This poses a risk for people with allergies to peanuts or tree nuts.
The bread products were made using wheat gluten that was previously recalled for containing undeclared peanut and/or tree nut residue. This means individuals with allergies to peanuts or tree nuts could experience an allergic reaction if they consume the product.
People with peanut or tree nut allergies who consume the recalled bread products are at risk. The recall affects specific bread items sold in the U.S. by Epi De France.
Check for the product names: '12" French Sub-roll' (36 count per case) or '12" Unsliced French Hoagie' (45 count per case). The products were sold by Epi De France in the U.S. with reference numbers 10048, 10943, and 10947.
Look for the product names '12" French Sub-roll' (36 count per case) or '12" Unsliced French Hoagie' (45 count per case) on the packaging.
The affected products are Epi breads, 12" French Sub-roll (36 count per case) and 12" Unsliced French Hoagie (45 count per case).
The bread products contain undeclared peanut and/or tree nut residue from wheat gluten that was previously recalled.
No specific action is required beyond checking product labels; the recall does not require immediate disposal.
We’ve drafted a message you can send Epi De France to request your refund or repair — edit it as you like.
Subject: Recall F-2745-2015 — Epi De France Epi De France Hello, I own a Epi De France that is covered by recall F-2745-2015 from Epi De France. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
